A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055760



Internal ID18798291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36001422..36062566hg38UCSC Ensembl
Innerchr17:34328461..34389926hg19UCSC Ensembl
Innerchr17:31352574..31414039hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3861145
hg1961466
hg1861466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561118
Samples
Known GenesCCL15, CCL15-CCL14, CCL23
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055760
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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